GUDIDData
gudid Primary ID: 18-01025-0601

Perfect Fit (UDI 18-01025-0601)

Manufactured by DYMEDIX DIAGNOSTICS, INC.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Perfect Fit - Primary ID 18-01025-0601

Device Regulatory Overview

The Perfect Fit (Model/Catalog Number: 18-01025-0601) is a medical device manufactured by DYMEDIX DIAGNOSTICS, INC.. This product is indexed under FDA Product Code / Category Classification BZQ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
18-01025-0601
Product Code / EMDN
BZQ
Device Name
FastTrack Starter Kit, Adult, NOX-T3
Database Sync Date
2026-08-09 09:31:20

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Perfect Fit?

The registered manufacturer of record for Perfect Fit is DYMEDIX DIAGNOSTICS, INC..

What is the Primary UDI-DI identifier for Perfect Fit?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 18-01025-0601.

What classification code is assigned to this device?

This device is registered under product classification code BZQ.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint